Human class V alcohol dehydrogenase (ADH5):: A complex transcription unit generates C-terminal multiplicity

被引:13
作者
Strömberg, P [1 ]
Höög, JO [1 ]
机构
[1] Karolinska Inst, Dept Med Biochem & Biophys, SE-17177 Stockholm, Sweden
关键词
human alcohol dehydrogenase; fetal; tissue; mRNA processing; polyadenylation; alternative splicing;
D O I
10.1006/bbrc.2000.3837
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The human ADH5 gene was reported to lack. the last exon compared to other mammalian ADHs and consequently should be expressed as a truncated protein. Here we show with PCR amplification of 3'-cDNA ends that the ADH5 gene harbors the "missing" exon. Besides a cDNA identical to the published sequence, we found full-length transcripts that contained additional codons for eight amino acid residues. Northern blot analysis established the full-length variant as the major transcript with the strongest signal from adult liver. Sequence analysis of genomic DNA confirmed that the ADH5 gene displays composite internal/terminal exons, which can be differentially processed; i.e., 3'-end generation is a result of competition between polyadenylation and splicing. (C) 2000 Academic Press.
引用
收藏
页码:544 / 549
页数:6
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